DEAH box RNA helicase DHX38 associates with satellite I noncoding RNA involved in chromosome segregation.
chromosome segregation
noncoding RNA
ribonucleoprotein (RNP) complex
Journal
Genes to cells : devoted to molecular & cellular mechanisms
ISSN: 1365-2443
Titre abrégé: Genes Cells
Pays: England
ID NLM: 9607379
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
11
03
2019
revised:
29
05
2019
accepted:
01
06
2019
pubmed:
6
6
2019
medline:
10
1
2020
entrez:
6
6
2019
Statut:
ppublish
Résumé
Noncoding (nc) RNA called satellite I is transcribed from the human centromere region. Depletion of this ncRNA results in abnormal nuclear morphology because of defects in chromosome segregation. Some protein factors interact with this ncRNA and function as a component of a nc ribonucleoprotein (RNP) complex in mitotic regulation. Here, we found that DHX38, a pre-mRNA splicing-related DEAH box RNA helicase, interacts with satellite I ncRNA. Depletion of DHX38 resulted in defective chromosome segregation similar to knockdown of satellite I ncRNA. Interaction between DHX38 and ncRNA was interphase-specific, but DHX38 depletion affected the function of Aurora B, which associated with satellite I ncRNA at mitotic phase. Based on these findings, we suggest that DHX38 has a role in mitotic regulation as a component of the satellite I ncRNP complex at interphase.
Substances chimiques
DNA, Satellite
0
RNA Splicing Factors
0
RNA, Untranslated
0
DHX38 protein, human
EC 3.6.1.-
DEAD-box RNA Helicases
EC 3.6.4.13
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
585-590Subventions
Organisme : The Ministry of Education, Culture, Sports, Science and Technology (MEXT)
ID : 26870442
Organisme : The Ministry of Education, Culture, Sports, Science and Technology (MEXT)
ID : 24770168
Organisme : The Ministry of Education, Culture, Sports, Science and Technology (MEXT)
ID : 23112716
Organisme : The Japan Agency for Medical Research and Development (CREST)
ID : JP16gm0510007
Informations de copyright
© 2019 Molecular Biology Society of Japan and John Wiley & Sons Australia, Ltd.